Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP751005.RA_deQcXZWat1bUXbNlVT5I-FhmZuS5AJtO_q1EJmSdGs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP751005.RA_deQcXZWat1bUXbNlVT5I-FhmZuS5AJtO_q1EJmSdGs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP751005.RA_deQcXZWat1bUXbNlVT5I-FhmZuS5AJtO_q1EJmSdGs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP751005.RA_deQcXZWat1bUXbNlVT5I-FhmZuS5AJtO_q1EJmSdGs130_provenance.
- NP751005.RA_deQcXZWat1bUXbNlVT5I-FhmZuS5AJtO_q1EJmSdGs130_assertion description "[NUP98-HOXD13 (NHD13) fusions have been identified in patients with myelodysplastic syndrome, acute myelogenous leukemia and chronic myeloid leukemia blast crisis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP751005.RA_deQcXZWat1bUXbNlVT5I-FhmZuS5AJtO_q1EJmSdGs130_provenance.
- NP751005.RA_deQcXZWat1bUXbNlVT5I-FhmZuS5AJtO_q1EJmSdGs130_assertion evidence source_evidence_literature NP751005.RA_deQcXZWat1bUXbNlVT5I-FhmZuS5AJtO_q1EJmSdGs130_provenance.
- NP751005.RA_deQcXZWat1bUXbNlVT5I-FhmZuS5AJtO_q1EJmSdGs130_assertion SIO_000772 17377591 NP751005.RA_deQcXZWat1bUXbNlVT5I-FhmZuS5AJtO_q1EJmSdGs130_provenance.
- NP751005.RA_deQcXZWat1bUXbNlVT5I-FhmZuS5AJtO_q1EJmSdGs130_assertion wasDerivedFrom befree-20140225 NP751005.RA_deQcXZWat1bUXbNlVT5I-FhmZuS5AJtO_q1EJmSdGs130_provenance.
- NP751005.RA_deQcXZWat1bUXbNlVT5I-FhmZuS5AJtO_q1EJmSdGs130_assertion wasGeneratedBy ECO_0000203 NP751005.RA_deQcXZWat1bUXbNlVT5I-FhmZuS5AJtO_q1EJmSdGs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP751005.RA_deQcXZWat1bUXbNlVT5I-FhmZuS5AJtO_q1EJmSdGs130_provenance.